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Nk-O3MD

by Narishige Lifemed Co., Ltd.

Ref 050

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number458981802MnpSy02Y3 Basic UDI-DI 04589818020500UDI-DIDate21 May 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Micromanipulator 02
Model / Reference
050
Primary DI / UDI-DI
04589818020500
Basic UDI-DI
458981802MnpSy02Y3
EMDN Code
U08020380 Devices for micromanipulation of biological material for assisted reproduction - accessories
Device Class
Class I
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
JP-MF-000033180
Authorised representative
Narishige International Limited NL-AR-000031466

Other devices from Narishige Lifemed Co., Ltd

See all devices from Narishige Lifemed Co., Ltd →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No